@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_head
{
this:
np:hasAssertion
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_assertion
;
np:hasProvenance
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_assertion
a
np:Assertion
.
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_provenance
a
np:Provenance
.
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0023267
a
ncit:C7057
.
dgn-gda:DGNf6f73847751bbe192d0891fb025d1b7e
sio:SIO_000628
miriam-gene:1543
,
lld:C0023267
;
a
sio:SIO_001121
.
}
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_provenance
{
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_assertion
dcterms:description
"[We concluded that the carriage of CYP1A1 Ile462Val AG and CYP1B1 Leu 432Val CC genotypes predict the susceptibility to leiomyoma in Egyptian women and they are likely to contribute in the pathogenesis of leiomyoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20559649
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP261645.RANueybCq7vLXh3FRt66nIbTUFuHsttZtUSTkLw1T_aNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}